EP0342036A1 - Silicate binders - Google Patents
Silicate binders Download PDFInfo
- Publication number
- EP0342036A1 EP0342036A1 EP19890304783 EP89304783A EP0342036A1 EP 0342036 A1 EP0342036 A1 EP 0342036A1 EP 19890304783 EP19890304783 EP 19890304783 EP 89304783 A EP89304783 A EP 89304783A EP 0342036 A1 EP0342036 A1 EP 0342036A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- silicate
- lithium
- welding
- binder
- lithium silicate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000011230 binding agent Substances 0.000 title claims abstract description 22
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 title claims abstract description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 45
- 238000003466 welding Methods 0.000 claims abstract description 29
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052912 lithium silicate Inorganic materials 0.000 claims abstract description 24
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 17
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 9
- 229910052681 coesite Inorganic materials 0.000 claims abstract description 8
- 229910052906 cristobalite Inorganic materials 0.000 claims abstract description 8
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 claims abstract description 8
- 229910052682 stishovite Inorganic materials 0.000 claims abstract description 8
- 229910052905 tridymite Inorganic materials 0.000 claims abstract description 8
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims description 12
- 239000004576 sand Substances 0.000 claims description 10
- 239000000017 hydrogel Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 239000003517 fume Substances 0.000 abstract description 20
- 239000011651 chromium Substances 0.000 abstract description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052804 chromium Inorganic materials 0.000 abstract description 7
- 150000004760 silicates Chemical class 0.000 abstract description 5
- 239000000203 mixture Substances 0.000 description 9
- 229910052744 lithium Inorganic materials 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229910000619 316 stainless steel Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
- -1 lithium silicates Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- KSPIHGBHKVISFI-UHFFFAOYSA-N Diphenylcarbazide Chemical compound C=1C=CC=CC=1NNC(=O)NNC1=CC=CC=C1 KSPIHGBHKVISFI-UHFFFAOYSA-N 0.000 description 1
- 229910000604 Ferrochrome Inorganic materials 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- PSHMSSXLYVAENJ-UHFFFAOYSA-N dilithium;[oxido(oxoboranyloxy)boranyl]oxy-oxoboranyloxyborinate Chemical compound [Li+].[Li+].O=BOB([O-])OB([O-])OB=O PSHMSSXLYVAENJ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010423 industrial mineral Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
- 238000004846 x-ray emission Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/20—Silicates
- C01B33/32—Alkali metal silicates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/36—Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
- B23K35/365—Selection of non-metallic compositions of coating materials either alone or conjoint with selection of soldering or welding materials
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B12/00—Cements not provided for in groups C04B7/00 - C04B11/00
- C04B12/04—Alkali metal or ammonium silicate cements ; Alkyl silicate cements; Silica sol cements; Soluble silicate cements
Definitions
- This invention relates to lithium silicate binder solutions which are of value in the manufacture, as examples, of welding rods and sand moulds.
- Silicates are well characterised in the literature, for example 'The Chemistry of Silica' by R K Iler (published by Wiley Interscience 1979), and they have a number of applications as binders. Examples of these applications are in sand moulding for metal casting, protective coatings, sealants, adhesives and as welding rod binders.
- silicate binder is required to provide mechanical strength to the formulation around the metal core and have a satisfactory moisture resistance.
- the invention provides a lithium silicate capable of acting as the sole silicate binder in welding rod compositions, sand moulds and the like and having a SiO2: Li2O weight ratio from about 7.5 to about 9:1.
- This silicate also provides sand moulds for casting having a particularly good strength.
- This lithium silicate is preferably obtained as solutions with the properties: Specific gravity @ 20°C 1.19 to 1.21 Lithium oxide 2.4 to 2.6% w/w Silica 20.1 to 21.0% w/w Weight ratio SiO2:Li2O 7.5 to 9:1 Solids content 22% to 26% wt
- the solids content is from about 18%, preferably from about 22%, to about 26% by weight. Above 26% the solution becomes too viscous to use and below 18% the solution does not act as an efficient binder.
- the invention extends to a method of preparing lithium silicate as defined wherein silica hydrogel is mixed with lithium hydroxide solution, preferably under conditions of shear, at a temperature not above about 35°C.
- the lump silica hydrogel used in the process is obtained from an acid/silicate reaction, for example as disclosed in GB 1215928 (Unilever), and may contain from about 5% to about 80% by weight silica, more usually about 20% to about 50%.
- lithium silicate of the defined wieght ratio provides welding rods of desired strength and water resistance without the requirement to have another soluble silicate present which would give rise to chromium fumes.
- the use of the lithium silicate of the invention as the sole silicate binder also reduces the total fume evolved during welding.
- GB 1532847 van Bearle
- Preparation of a silicates mixture by dissolving silica hydrogel in silicate solution and then admixing lithium hydroxide is provided in US 3522066 (Lithium Corp).
- the applications for lithium silicates have been generally described in Electrical Manufacture September 1964.
- GB 1183120 (Henkel) describes preparation of lithium silicates by mixing silicic acid and lithium hydroxide solution at a temperature above 80°C.
- GB 1581182 (Kobe Steel) is directed to the problem of chromium fumes in welding but teaches the use of specified oxides in colloidal form in the binder.
- This silicate solution is prepared by dissolving lithium hydroxide monohydrate in demineralised water (1163 mls at 20°C) with constant stirring for 15 minutes using a high speed agitator (Moritz obtained from Moritz Chemical Engineering Congress, England). Acid washed silica hydrogel lumps (33% solids) was then added in two stages with stirring. Half was added over 15 minutes and the solution allowed to stand for 10 minutes before adding the remainder of the hydrogel over 20 minutes. Stirring was continued for up to 3 hours before the final product was available for use.
- Lithium silicate solution from these four batches was used as binder in the preparation of welding rods standard compositions and methods described by J. Griffiths in Industrial Minerals March 1985.
- the electrodes tested were Babcock 'S' 316L Regular (electrode A) (obtainable from Babcock Welding Products Ltd of England) and an equivalent electrode using lithium silicate solution of the invention as the sole silicate binder (electrode B).
- a comparison electrode (D) was prepared using the lithium silicate V and tested together with a standard electrode (C) (Babcock standard S1). These electrodes were stainless steel manual metal are electrodes have a diameter of 3.25 mm. All tests were performed on horizontal-vertical fillets which were 250 mm long and made from 50 mm x 10 mm Type 316 stainless steel.
- Welding was carried out at approximately 120 amps DC positive (Table 1). Each test consisted of welding a horizontal-vertical fillet using an arc length determined by the welder as being 'normal' for the electrode under investigation. Voltage, current and arcing time were measured electronically using The Welding Institute system (Welding Institute Research Bulletin vol. 25 No. 1 (Janaury 1984) p14).
- Fume samples for emission rate tests were collected on glass fibre filters (Type GF/C 240 mm diameter), which were weighed before and after welding to determine the weight of fume collected. The weight of deposited weld metal was also determined. A Swedish fume box was used for the tests, this fume box is described in Welding Institute Research Bulletin vo. 25 No. 7 July 1984 p230 and International Institute of Welding doc 11E-233-77.
- the principle analytical technique for the collected fumes was X-ray fluorescence spectrometry.
- 1g sample was fused with a mixture of 2g lanthanum oxide and 9g lithium tetraborate at 1200°C for 12 minutes.
- the resulting fusion mixture was cast into a bead of suitable size for analysis.
- Hexavalent chromium was analysed using a spectrophotometric method employing s-diphenyl carbazide as a colour reagent.
- Table II shows the fume emission rate results, together with relevant welding parameters and an indication of the number of tests performed.
- a typical welding rod formulation intended for forming round a cylindrical stainless steel rod, contains (parts by weight): Ferrochrome alloy powder 13.5 rutile 36 feldspa 13.5 calcium carbonate 22.5 sodium carboxymethyl cellulose 4.5 lithium silicate of invention 10.0 100.0
- the utility of the lithium silicate of the invention for sand moulding was demonstrated by adding 150g of one of the batches to sand (1Kg) and mixing thoroughly for 1 minute.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Nonmetallic Welding Materials (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
- This invention relates to lithium silicate binder solutions which are of value in the manufacture, as examples, of welding rods and sand moulds.
- Silicates are well characterised in the literature, for example 'The Chemistry of Silica' by R K Iler (published by Wiley Interscience 1979), and they have a number of applications as binders. Examples of these applications are in sand moulding for metal casting, protective coatings, sealants, adhesives and as welding rod binders.
- In the latter application the silicate binder is required to provide mechanical strength to the formulation around the metal core and have a satisfactory moisture resistance.
- Additionally, the effect of binder composition on the evolution of chromium fumes during welding has been described by Kimura et al in a paper presented to the American Welding Society in April 1979 and published in Welding Research Supplement July 1979. The chromium fumes can arise from both the substrate and rod and Kimura demonstrated that reducing the sodium and potassium level in the water soluble binder component leads to a reduction in evolution of chromium fumes while the presence of lithium did not lead to chromium evolution. Thus there is an advantage in using only lithium silicate as the rod binder.
- A general background description of welding can be found in Kirk Othner (pub. Wiley & Son 1970) vol 22 pages 241 to 252. Although the term welding 'rod' is used herein it will be understood that the welding electrode used may have a shape other than the geometric rod.
- The invention provides a lithium silicate capable of acting as the sole silicate binder in welding rod compositions, sand moulds and the like and having a SiO₂: Li₂O weight ratio from about 7.5 to about 9:1. This silicate also provides sand moulds for casting having a particularly good strength. This lithium silicate is preferably obtained as solutions with the properties:
Specific gravity @ 20°C 1.19 to 1.21 Lithium oxide 2.4 to 2.6% w/w Silica 20.1 to 21.0% w/w Weight ratio SiO₂:Li₂O 7.5 to 9:1 Solids content 22% to 26% wt - Preferably the solids content is from about 18%, preferably from about 22%, to about 26% by weight. Above 26% the solution becomes too viscous to use and below 18% the solution does not act as an efficient binder.
- The invention extends to a method of preparing lithium silicate as defined wherein silica hydrogel is mixed with lithium hydroxide solution, preferably under conditions of shear, at a temperature not above about 35°C. The lump silica hydrogel used in the process is obtained from an acid/silicate reaction, for example as disclosed in GB 1215928 (Unilever), and may contain from about 5% to about 80% by weight silica, more usually about 20% to about 50%.
- The applicants have found lithium silicate of the defined wieght ratio provides welding rods of desired strength and water resistance without the requirement to have another soluble silicate present which would give rise to chromium fumes. The use of the lithium silicate of the invention as the sole silicate binder also reduces the total fume evolved during welding.
- The use of a mixture of lithium, potassium and sodium silicates as a welding rod binder solution is described in GB 1532847 (van Bearle). Preparation of a silicates mixture by dissolving silica hydrogel in silicate solution and then admixing lithium hydroxide is provided in US 3522066 (Lithium Corp). The applications for lithium silicates have been generally described in Electrical Manufacture September 1964. GB 1183120 (Henkel) describes preparation of lithium silicates by mixing silicic acid and lithium hydroxide solution at a temperature above 80°C. GB 1581182 (Kobe Steel) is directed to the problem of chromium fumes in welding but teaches the use of specified oxides in colloidal form in the binder.
- Examples of the preparation of the lithium silicate of the invention and its application in welding and sand moulding will now be given to illustrate but not limit the invention.
- This silicate solution is prepared by dissolving lithium hydroxide monohydrate in demineralised water (1163 mls at 20°C) with constant stirring for 15 minutes using a high speed agitator (Moritz obtained from Moritz Chemical Engineering Kingston upon Thames, England). Acid washed silica hydrogel lumps (33% solids) was then added in two stages with stirring. Half was added over 15 minutes and the solution allowed to stand for 10 minutes before adding the remainder of the hydrogel over 20 minutes. Stirring was continued for up to 3 hours before the final product was available for use.
- Four batches of the silicate solution were prepared with the amounts of reactants and properties given in Table I together with a comparative lithium silicate solution (V) of higher ratio.
TABLE I BATCH I II III IV V LiOH.H₂O (g) 240 255 260 290 119 Silica Hydrogel (g) 2173 2375 2140 2460 1450 Total solids 22.42 23.46 22.84 23.73 19.05 Li₂O(%wt) 2.37 2.39 2.60 2.65 1.55 SiO₂(%wt) 20.05 21.07 20.24 21.08 17.50 Weight ratio 8.46 8.82 7.79 7.96 11.30 S. Gravity 1.1932 1.2003 1.1989 1.2074 1.15 - Lithium silicate solution from these four batches was used as binder in the preparation of welding rods standard compositions and methods described by J. Griffiths in Industrial Minerals March 1985.
- These rods had good structural strength and bonding, satisfactory water resistance and used lithium silicate as the sole water soluble silicate binder.
- The electrodes tested were Babcock 'S' 316L Regular (electrode A) (obtainable from Babcock Welding Products Ltd of England) and an equivalent electrode using lithium silicate solution of the invention as the sole silicate binder (electrode B). A comparison electrode (D) was prepared using the lithium silicate V and tested together with a standard electrode (C) (Babcock standard S1). These electrodes were stainless steel manual metal are electrodes have a diameter of 3.25 mm. All tests were performed on horizontal-vertical fillets which were 250 mm long and made from 50 mm x 10 mm Type 316 stainless steel.
- Welding was carried out at approximately 120 amps DC positive (Table 1). Each test consisted of welding a horizontal-vertical fillet using an arc length determined by the welder as being 'normal' for the electrode under investigation. Voltage, current and arcing time were measured electronically using The Welding Institute system (Welding Institute Research Bulletin vol. 25 No. 1 (Janaury 1984) p14).
- Fume samples for emission rate tests were collected on glass fibre filters (Type GF/C 240 mm diameter), which were weighed before and after welding to determine the weight of fume collected. The weight of deposited weld metal was also determined. A Swedish fume box was used for the tests, this fume box is described in Welding Institute Research Bulletin vo. 25 No. 7 July 1984 p230 and International Institute of Welding doc 11E-233-77.
- From the above it was possible to calculate fume emission rate using the units:
milligrams fume per second
milligrams fume per gram deposited weld metal. - Sufficient fume for analysis was collected on Whatman 41 paper filters by repeated welding. (Paper filter, in preference to glass filters, were used because of their low blank value).
- The principle analytical technique for the collected fumes was X-ray fluorescence spectrometry. In this case 1g sample was fused with a mixture of 2g lanthanum oxide and 9g lithium tetraborate at 1200°C for 12 minutes. The resulting fusion mixture was cast into a bead of suitable size for analysis.
- Hexavalent chromium was analysed using a spectrophotometric method employing s-diphenyl carbazide as a colour reagent.
- Table II shows the fume emission rate results, together with relevant welding parameters and an indication of the number of tests performed. Thus use of lithium silicate as the sole silicate binder reduces the Cr V1 emission but use of a lithium silicate according to the present invention also reduces the total fume emission.
- A typical welding rod formulation, intended for forming round a cylindrical stainless steel rod, contains (parts by weight):
Ferrochrome alloy powder 13.5 rutile 36 feldspa 13.5 calcium carbonate 22.5 sodium carboxymethyl cellulose 4.5 lithium silicate of invention 10.0 100.0 - Incorpiration of the lithium silicate of the invention may require some variation in the coating process, e.g. baking, but these variations can be identified by experimentation.
TABLE II WELDING PARMETERS AND FUME EMISSION RATES Electrode No Tests Welding Parameters Fume Emission Rates Polarity OCV Current A Volts V Mean mg/s Mean mg/g deposit Cr V1 A 5 DC+ 80 118 23 3.5 11.7 4.9 B 5 DC+ 80 117 24 1.6 4.7 0.5 C 5 DC+ 80 134 26 4.6 12.6 5.3 D 6 DC+ 80 132 30 4.4 12.2 0.1 - The utility of the lithium silicate of the invention for sand moulding was demonstrated by adding 150g of one of the batches to sand (1Kg) and mixing thoroughly for 1 minute.
- A portion was then placed in a mould, compressed three times and the green strength measured. A number of cores were made and heated at various temperatures, from 58°C to 350°C, for 1 hour. The cores were allowed to cool overnight and the strength then measured. The results given in Table III demonstrate the lithium silicate binder provides satisfactory core strengths.
TABLE III Temp (°C) Green 58 100 125 150 200 250 300 350 Core Strength (lbs per sq in)1 160 260 930 320 210 170 140 150
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT89304783T ATE95455T1 (en) | 1988-05-13 | 1989-05-11 | SILICATE BINDER. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8811411 | 1988-05-13 | ||
GB888811411A GB8811411D0 (en) | 1988-05-13 | 1988-05-13 | Silicate binders |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0342036A1 true EP0342036A1 (en) | 1989-11-15 |
EP0342036B1 EP0342036B1 (en) | 1993-10-06 |
Family
ID=10636884
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89304783A Expired - Lifetime EP0342036B1 (en) | 1988-05-13 | 1989-05-11 | Silicate binders |
Country Status (10)
Country | Link |
---|---|
US (1) | US5151121A (en) |
EP (1) | EP0342036B1 (en) |
JP (1) | JPH02504264A (en) |
AT (1) | ATE95455T1 (en) |
AU (1) | AU3735089A (en) |
BR (1) | BR8906961A (en) |
DE (1) | DE68909669D1 (en) |
GB (1) | GB8811411D0 (en) |
WO (1) | WO1989010819A1 (en) |
ZA (1) | ZA893566B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2866825A1 (en) * | 2004-03-01 | 2005-09-02 | Air Liquide | HEXAVALENT SMOKE AND LOW SMOKE EMITTED ELECTRODE FOR STAINLESS STEEL WELDING |
EP1585980A1 (en) * | 2003-01-21 | 2005-10-19 | X-ray Flux Pty Ltd. | X-ray fluorescence flux composition |
EP3266560A1 (en) * | 2016-07-05 | 2018-01-10 | Ductil S.A. | Multi-coated electrode for welding stainless steel |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3180747A (en) * | 1961-08-03 | 1965-04-27 | Exxon Research Engineering Co | Protective coating |
US3392039A (en) * | 1964-12-17 | 1968-07-09 | Philadelphia Quartz Company Of | Lithium silicate composition |
CH472488A (en) * | 1965-04-02 | 1969-05-15 | Du Pont | Self-curing inorganic coating agent and process for its preparation |
US3522066A (en) * | 1966-12-06 | 1970-07-28 | Lithium Corp | Process for preparing aqueous mixed lithium and sodium (and/or potassium) silicate solutions |
US3533816A (en) * | 1965-10-22 | 1970-10-13 | Du Pont | Preparation of high ratio alkali metal silicates |
US3576597A (en) * | 1967-09-27 | 1971-04-27 | Philadelphia Quartz Co | Method for the preparation of lithium silicate solutions |
FR2332311A1 (en) * | 1975-11-18 | 1977-06-17 | Baerle Et Cie Ag Van | BINDER BASED ON AQUEOUS SOLUTIONS OF ALKALINE SILICATES, ITS OBTAINING AND ITS APPLICATIONS |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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-
1988
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-
1989
- 1989-05-11 US US07/460,875 patent/US5151121A/en not_active Expired - Fee Related
- 1989-05-11 BR BR898906961A patent/BR8906961A/en unknown
- 1989-05-11 AT AT89304783T patent/ATE95455T1/en not_active IP Right Cessation
- 1989-05-11 AU AU37350/89A patent/AU3735089A/en not_active Abandoned
- 1989-05-11 DE DE89304783T patent/DE68909669D1/en not_active Expired - Lifetime
- 1989-05-11 WO PCT/GB1989/000509 patent/WO1989010819A1/en unknown
- 1989-05-11 JP JP1505602A patent/JPH02504264A/en active Pending
- 1989-05-11 EP EP89304783A patent/EP0342036B1/en not_active Expired - Lifetime
- 1989-05-12 ZA ZA893566A patent/ZA893566B/en unknown
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1585980A1 (en) * | 2003-01-21 | 2005-10-19 | X-ray Flux Pty Ltd. | X-ray fluorescence flux composition |
EP1585980A4 (en) * | 2003-01-21 | 2008-07-30 | X Ray Flux Pty Ltd | X-ray fluorescence flux composition |
FR2866825A1 (en) * | 2004-03-01 | 2005-09-02 | Air Liquide | HEXAVALENT SMOKE AND LOW SMOKE EMITTED ELECTRODE FOR STAINLESS STEEL WELDING |
EP1570944A1 (en) * | 2004-03-01 | 2005-09-07 | La Soudure Autogene Francaise | Coated electrode with low gas emission and low hexavalent chromium, for welding stainless steel |
EP3266560A1 (en) * | 2016-07-05 | 2018-01-10 | Ductil S.A. | Multi-coated electrode for welding stainless steel |
WO2018007364A1 (en) * | 2016-07-05 | 2018-01-11 | Ductil Sa | Multi-coated electrode for welding stainless steel |
Also Published As
Publication number | Publication date |
---|---|
WO1989010819A1 (en) | 1989-11-16 |
ZA893566B (en) | 1991-01-30 |
GB8811411D0 (en) | 1988-06-15 |
BR8906961A (en) | 1990-11-20 |
EP0342036B1 (en) | 1993-10-06 |
AU3735089A (en) | 1989-11-29 |
JPH02504264A (en) | 1990-12-06 |
ATE95455T1 (en) | 1993-10-15 |
US5151121A (en) | 1992-09-29 |
DE68909669D1 (en) | 1993-11-11 |
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